Trials / Completed
CompletedNCT00004336
Pilot Study of Familial Nonsyndromal Mondini Dysplasia
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 2 (planned)
- Sponsor
- National Center for Research Resources (NCRR) · NIH
- Sex
- All
- Age
- 0 Years
- Healthy volunteers
- Not accepted
Summary
OBJECTIVES: I. Determine the mode of inheritance of nonsyndromal Mondini inner ear dysplasia, an inner ear malformation causing deafness, vestibular dysfunction, and recurrent meningitis.
Detailed description
PROTOCOL OUTLINE: The parents of 1 family with known Mondini dysplasia are screened for the disorder using temporal bone computerized tomography without contrast. This information is used to determine the mode of inheritance.
Conditions
Timeline
- Start date
- 1995-10-01
- First posted
- 1999-10-19
- Last updated
- 2005-06-24
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00004336. Inclusion in this directory is not an endorsement.